Canonical Allele Identifier: CA270618
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 143894
ClinVar RCV Id: RCV000133433
dbSNP Id: rs527236189
MyVariant Identifiers: chrMT:g.15553G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15553G>A , J01415.2:m.15553G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.807G>A ENSP00000354554.2:p.Lys269=